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Prof. Dr. Heinrich Sticht
List of publications:
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Professur für Bioinformatik
Award(s)
(1)
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(1)
Project Memberships
(3)
Publications
(253)
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Journal article
Journal article
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Assessing clinical utility of preconception expanded carrier screening regarding residual risk for neurodevelopmental disorders (2022)
Boonsawat P, Horn AHC, Steindl K, Baumer A, Joset P, Kraemer D, Bahr A, et al.
Journal article
Highly Conserved Interaction Profiles between Clinically Relevant Mutants of the Cytomegalovirus CDK-like Kinase pUL97 and Human Cyclins: Functional Significance of Cyclin H (2022)
Schütz M, Müller R, Socher E, Wangen C, Full F, Wyler E, Wong DD, et al.
Journal article
Media Modulation based Molecular Communication (2022)
Brand L, Garkisch M, Lotter S, Schäfer M, Burkovski A, Sticht H, Castiglione K, Schober R
Journal article
De Novo Missense Variants in SLC32A1 Cause a Developmental and Epileptic Encephalopathy Due to Impaired GABAergic Neurotransmission (2022)
Platzer K, Sticht H, Bupp C, Ganapathi M, Pereira EM, Le Guyader G, Bilan F, et al.
Journal article
A novel splice variant of Argonaut 2 affects microRNA target genes and cell viability of melanoma cells (2022)
Linck-Paulus L, Horn A, Matthies AO, Fischer S, Meister G, Sticht H, Kappelmann-Fenzl M, Boßerhoff AK
Conference contribution
A previously unknown Argonaute 2 variant positively modulates the viability of melanoma cells (2022)
Linck-Paulus L, Meißgeier T, Pieger K, Horn A, Matthies AO, Fischer S, Meister G, et al.
Journal article
A newly identified secreted larval antigen elicits basophil-dependent protective immunity against N. brasiliensis infection (2022)
Thuma N, Döhler D, Mielenz D, Sticht H, Radtke D, Reimann L, Warscheid B, Vöhringer D
Journal article
The recurrent TCF4 missense variant p.(Arg389Cys) causes a neurodevelopmental disorder overlapping with but not typical for Pitt-Hopkins syndrome (2022)
Popp B, Bienvenu T, Giurgea I, Metreau J, Kraus C, Reis A, Fischer J, et al.
Journal article
Bi-allelic loss-of-function variants in PPFIBP1 cause a neurodevelopmental disorder with microcephaly, epilepsy, and periventricular calcifications (2022)
Rosenhahn E, O'Brien TJ, Zaki MS, Sorge I, Wieczorek D, Rostasy K, Vitobello A, et al.
Journal article
Characterization of SARS-CoV-2 Escape Mutants to a Pair of Neutralizing Antibodies Targeting the RBD and the NTD (2022)
Peter AS, Grüner E, Socher E, Fraedrich K, Richel E, Müller-Schmucker S, Cordsmeier A, et al.
Journal article
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